1. Transient Activation of Autophagy via Sox2-Mediated Suppression of mTOR Is an Important Early Step in Reprogramming to Pluripotency 
Shuo Wang, Pengyan Xia, Buqing Ye, Guanling Huang, Jing Liu, Zusen Fan 
Cell Stem Cell 
Volume 13, Issue 5, Pages (November 2013)
DOI: /j.stem
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2. Cell Stem Cell 2013 13, 617-625DOI: (10.1016/j.stem.2013.10.005)
Copyright © 2013 Elsevier Inc. Terms and Conditions

3. Figure 1 Autophagy Is Essential for iPSC Generation
(A) Atg5 deficiency impairs iPSC formation. Atg5+/+ or Atg5−/− MEFs carrying drug-inducible OSKM factors (hereinafter referred to as 4F2A MEFs) were cultured in ESC media containing 2 μg/ml doxycycline for 3 weeks and detected for alkaline phosphatase (AP) activity (upper panel) or stained with anti-SSEA-1 antibody (lower panel). Colony numbers per 104 cells were calculated and shown as mean ± SD. ∗∗∗p <
(B) iPSCs from Atg5+/+, but not Atg5−/−; 4F2A MEFs, can form teratomas. Atg5+/+ or Atg5−/−; 4F2A MEFs treated as above were harvested and subcutaneously injected into NOD-SCID mice. One month later, teratomas were collected for H&E staining. EN, endoderm; ME, mesoderm; EC. ectoderm. Scale bar, 200 μm.
(C) Autophagy in iPSC formation. GFP-LC3; 4F2A MEFs were treated with doxycycline for the indicated days and immunostained by anti-Sox2 antibody. Nuclei were visualized by DAPI. GFP-LC3 dots per cell were calculated and shown as mean ± SD. ∗∗p < 0.01; ∗∗∗p < Scale bar, 10 μm.
(D) Autophagic flux during iPSC generation. WT 4F2A MEFs were treated with doxycycline for the indicated days and harvested for immunoblotting.
(E) Autophagosomal structures appear during iPSC generation. WT 4F2A MEFs were cultured in doxycycline-contained ESC media and autophagosomes were analyzed by electron microscopy and shown as mean ± SD. ∗∗p < 0.01; ∗∗∗p < Red arrowhead indicates autophagosome. Scale bar, 500 nm.
(F) Autophagy is enhanced at the four- to eight-cell stage during embryonic development. Embryos at the indicated stages from GFP-LC3 transgenic mice were isolated, and cultured in OSKM media with or without 20 nM Bafilomycin A1 (BafA1) for 4 hr, and visualized by confocal microscopy. Scale bar, 20 μm.
(G) Rapamycin promotes reprogramming of embryos. Embryos were isolated at embryo day (E) 1.5 and cultured in OSKM media. One microgram per milliliter of rapamycin was added into culture at E2.5 for 4 hr. Distribution of embryonic stage at E3.0 was calculated as mean ± SD (right panel). ∗∗p < Red arrow indicates blastocyst. Scale bar, 100 μm.
See also Figure S1.
Cell Stem Cell  , DOI: ( /j.stem )
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4. Figure 2
Sox2 Contributes to Autophagy Initiation during iPSC Formation
(A) Sox2 downregulates mTOR mRNA during iPSC formation. WT MEFs were infected with retrovirus encoding OSKM factors together or individually and cultured in ESC media for 24 hr. mRNA levels of the indicated genes were analyzed by RT-PCR. Data are representative of three different experiments and shown as mean ± SD. ∗∗p < 0.01.
(B) Sox2 contributes to mTOR repression. WT MEFs treated as above were harvested and subjected to immunoblotting with the indicated antibodies.
(C) Sox2 initiates autophagy. GFP-LC3 MEFs were infected with retrovirus encoding Sox2 or empty vector (Ctrl) and cultured in ESC media for 48 hr, and GFP-LC3 dots were analyzed by confocal microscopy (upper panel) and calculated as mean ± SD (lower panel). ∗∗∗p < Scale bar, 10 μm.
(D) mTOR is downregulated at the four- to eight-cell stage of embryos. Embryos at the indicated stages were isolated and subjected to immunostaining. Nuclei were visualized by DAPI. Scale bar, 20 μm.
(E) Transcription of mTOR is impaired at the four- to eight-cell stage. Embryos at the two-cell stage (E1.5) or the four- to eight-cell stage (E2.5) were isolated and harvested for mRNA extraction for RT-PCR. Data are representative of three independent experiments and are shown as mean ± SD.
(F) Autophagy is defective in Sox2−/− embryos. Embryos from Sox2+/−; EIIa-Cre; GFP-LC3 females mated with Sox2flox/+ males were isolated for immunostaining. Scale bar, 20 μm.
(G) Sox2 deficiency potentiates mTOR expression. Embryos from Sox2+/−; EIIa-Cre females mated with Sox2flox/+ males were harvested for immunostaining. Scale bar, 20 μm. We used two different anti-mTOR antibodies (#2972 and #2983, Cell Signaling Technology) for immunoblotting and two different anti-mTOR antibodies (#2983 from Cell Signaling Technology and #sc-8319 from Santa Cruz Biotechnology) for immunofluorescent staining and received similar results.
See also Figure S2.
Cell Stem Cell  , DOI: ( /j.stem )
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5. Figure 3 Sox2 Targets mTOR Promoter to Repress Its Expression
(A) Sox2 is recruited to the mTOR promoter. ChIP analysis monitored binding of Sox2 to mTOR promoter in MEFs expressing empty vector (Ctrl) or Sox2. Data represent at least three separate experiments and are shown as mean ± SD. ∗∗p < 0.01.
(B and C) Sox2 suppresses mTOR transcription. Different loci of the mTOR promoter were constructed into pGL3 vector, transfected into MEFs expressing empty vector (Ctrl) or Sox2, and subjected to luciferase reporter assay. Data are representative of three different experiments and are shown as mean ± SD. ∗∗p < 0.01.
(D) Sox2 binds to the mTOR promoter. Nuclear extracts from MEFs expressing Sox2 were monitored by EMSA assay with different probes as shown in the upper panel.
(E) Sox2 binds a specific locus on the mTOR promoter. EMSA assay monitored Sox2 binding of mTOR promoter with the specific 40 nucleotide probe (#2 probe as in 3D) with nuclear extracts from MEFs expressing empty vector (Ctrl) or Sox2. Anti-Sox2 antibody was added for supershift assay, and unlabeled probes were added for competitive reaction.
(F) The repressive locus deletion (ΔmTOR) abolishes Sox2 binding to mTOR promoter. WT or ΔmTOR MEFs expressing empty vector (Ctrl) or Sox2 were subjected to ChIP assay by our use of anti-Sox2 antibody. Data are representative of three independent experiments and are shown as mean ± SD. ∗∗p < 0.01.
(G) ΔmTOR abrogates mTOR downregulation and autophagy. WT or ΔmTOR; 4F2A MEFs were cultured in doxycycline-contained ESC media for the indicated days and harvested for immunoblotting.
(H) mTOR expression and autophagy induction are impaired in ΔmTOR MEFs. WT or ΔmTOR; GFP-LC3; 4F2A MEFs were cultured in doxycycline-contained ESC media for 48 hr and subjected to immunostaining. Scale bar, 10 μm.
(I) iPSC generation is blocked in ΔmTOR MEFs. 4F2A WT or 4F2A; ΔmTOR MEFs were treated with or without 1 μg/ml rapamycin (Rapa) for 48 hr and cultured in ESC media containing doxycycline for 3 weeks. The iPSCs were visualized by AP staining. Data are representative of three different experiments and are shown as mean ± SD. ∗∗∗p < Similar results were obtained by using two different anti-mTOR antibodies for immunoblotting and immunofluorescence assays as described above.
See also Figure S3.
Cell Stem Cell  , DOI: ( /j.stem )
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6. Figure 4 Sox2 Recruits the NuRD Complex to Inhibit mTOR Transcription
(A) Identification of NuRD complex by a DNA pulldown assay. The binding region (40 nt) on the mTOR promoter of Sox2 was conjugated to CNBr activated beads. Nuclear extracts from MEFs expressing GFP or Sox2 were incubated with DNA-conjugated beads for 20 min and the precipitates were subjected to SDS-PAGE for silver staining and mass spectrometry. M, molecular weight (MW) marker.
(B) The identified components of the NuRD complex were confirmed by western blotting.
(C) Sox2 can precipitate the NuRD complex in vivo. MEFs expressing GFP or Sox2 were harvested for immunoprecipitation with anti-Sox2 antibody. Immunoprecipitates were detected by immunoblotting with the indicated antibodies.
(D) Silencing of NuRD complex components restores mTOR mRNA levels. MEFs were infected with retrovirus encoding shRNA against scramble sequence (shCtrl) or components of NuRD complex, as well as Sox2 or empty vector, and cultured in ESC media for 24 hr followed by RT-PCR analysis. Data are representative of at least three experiments and are shown as mean ± SD. ∗∗p < 0.01.
(E) The NuRD complex is required for autophagy flux induced by Sox2. MEFs were infected with retrovirus encoding the indicated shRNA and Sox2 or empty vector, cultured in ESC media for 24 hr, and harvested for immunoblotting. β-actin was used as a loading control.
(F) The NuRD complex is recruited to mTOR promoter during early embryonic development. Embryos from the two-cell stage or the four- to eight-cell stage were determined by ChIP analysis. Data represent three separate experiments and are shown as mean ± SD. ∗∗p < 0.01.
(G and H) Knockdown of NuRD complex components impairs mTOR downregulation at the four- to eight-cell stage of embryos. Mi-2β (G) or LSD1 (H) was silenced with siRNA duplexes at E1.5. Embryos were cultured in OSKM media for 24 hr and subjected to immunostaining. Scale bar, 20 μm. Similar results were obtained by using two different anti-mTOR antibodies for immunoblotting and immunofluorescence assays as described above.
See also Figure S4.
Cell Stem Cell  , DOI: ( /j.stem )
Copyright © 2013 Elsevier Inc. Terms and Conditions